纳米载体
抗菌剂
生物物理学
介孔二氧化硅
细菌
微生物代谢
纳米技术
化学
生物化学
纳米颗粒
生物膜
控制释放
材料科学
组合化学
代谢途径
纳米毒理学
前药
药品
药物输送
新陈代谢
硫酸化
内化
抗菌肽
靶向给药
肽
纳米材料
群体感应
微生物群
微生物学
药物发现
介孔材料
作者
Jianhui Liu,Jeremy Elias,Xiaohong Wang,Jing Tian,Pu‐Ting Dong,Huilin Cao,Lujia Cen,Mohammed Zahedul Islam Nizami,Xuesong He,Jirun Sun
标识
DOI:10.1021/acsami.6c05401
摘要
Abstract Acidogenic and aciduric bacteria acidify their local microenvironment through carbohydrate metabolism, contributing to pathological microenvironment acidification in diseases, including dental caries, infection, and inflammation. We present a mesoporous silica nanoparticle platform equipped with surface-bound, pH-responsive gatekeepers that remain sealed at physiological pH yet rapidly release a drug payload under acidic conditions. This system converts a broad-spectrum antimicrobial into a selectively activated antimicrobial system: release is suppressed under neutral conditions and triggered when bacteria generate acid. In a human oral microbiome model, the nanoparticles selectively eradicate acid-producing bacteria, with metabolic acidification directly activating their own killing, as evidenced by simultaneous single-cell-scale fluorescence imaging of pH and viability. Mechanistic studies using proton NMR and contact angle measurements show that the gating mechanism relies on synergistic molecular interactions and hydrophilicity–hydrophobicity transitions. This work establishes an on-site antimicrobial strategy triggered by metabolic acidification for targeting microbes with undesirable metabolic features, thus paving the way toward more controlled infection therapies.
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